-
1
-
-
34548441098
-
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution
-
Bignell G.R., Santarius T., Pole J.C., et al. Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution. Genome Res 2007, 17:1296-1303.
-
(2007)
Genome Res
, vol.17
, pp. 1296-1303
-
-
Bignell, G.R.1
Santarius, T.2
Pole, J.C.3
-
2
-
-
43049143055
-
Mapping and sequencing of structural variation from eight human genomes
-
Kidd J.M., Cooper G.M., Donahue W.F., et al. Mapping and sequencing of structural variation from eight human genomes. Nature 2008, 453:56-64.
-
(2008)
Nature
, vol.453
, pp. 56-64
-
-
Kidd, J.M.1
Cooper, G.M.2
Donahue, W.F.3
-
3
-
-
22844451617
-
Fine-scale structural variation of the human genome
-
Tuzun E., Sharp A.J., Bailey J.A., et al. Fine-scale structural variation of the human genome. Nat Genet 2005, 37:727-732.
-
(2005)
Nat Genet
, vol.37
, pp. 727-732
-
-
Tuzun, E.1
Sharp, A.J.2
Bailey, J.A.3
-
4
-
-
33644653015
-
Decoding the fine-scale structure of a breast cancer genome and transcriptome
-
Volik S., Raphael B.J., Huang G., et al. Decoding the fine-scale structure of a breast cancer genome and transcriptome. Genome Res 2006, 16:394-404.
-
(2006)
Genome Res
, vol.16
, pp. 394-404
-
-
Volik, S.1
Raphael, B.J.2
Huang, G.3
-
5
-
-
0037934515
-
End-sequence profiling: sequence-based analysis of aberrant genomes
-
Volik S., Zhao S., Chin K., et al. End-sequence profiling: sequence-based analysis of aberrant genomes. Proc Natl Acad Sci U S A 2003, 100:7696-7701.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 7696-7701
-
-
Volik, S.1
Zhao, S.2
Chin, K.3
-
6
-
-
55549089660
-
Accurate whole human genome sequencing using reversible terminator chemistry
-
Bentley D.R., Balasubramanian S., Swerdlow H.P., et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 2008, 456:53-59.
-
(2008)
Nature
, vol.456
, pp. 53-59
-
-
Bentley, D.R.1
Balasubramanian, S.2
Swerdlow, H.P.3
-
7
-
-
44349191457
-
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
-
Campbell P.J., Stephens P.J., Pleasance E.D., et al. Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing. Nat Genet 2008, 40:722-729.
-
(2008)
Nat Genet
, vol.40
, pp. 722-729
-
-
Campbell, P.J.1
Stephens, P.J.2
Pleasance, E.D.3
-
8
-
-
35348988679
-
Paired-end mapping reveals extensive structural variation in the human genome
-
Korbel J.O., Urban A.E., Affourtit J.P., et al. Paired-end mapping reveals extensive structural variation in the human genome. Science 2007, 318:420-426.
-
(2007)
Science
, vol.318
, pp. 420-426
-
-
Korbel, J.O.1
Urban, A.E.2
Affourtit, J.P.3
-
9
-
-
68149176840
-
Chimeric transcript discovery by paired-end transcriptome sequencing
-
Maher C.A., Palanisamy N., Brenner J.C., et al. Chimeric transcript discovery by paired-end transcriptome sequencing. Proc Natl Acad Sci U S A 2009, 106:12353-12358.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 12353-12358
-
-
Maher, C.A.1
Palanisamy, N.2
Brenner, J.C.3
-
10
-
-
69749090013
-
Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding
-
McKernan K.J., Peckham H.E., Costa G.L., et al. Sequence and structural variation in a human genome uncovered by short-read, massively parallel ligation sequencing using two-base encoding. Genome Res 2009, 19:1527-1541.
-
(2009)
Genome Res
, vol.19
, pp. 1527-1541
-
-
McKernan, K.J.1
Peckham, H.E.2
Costa, G.L.3
-
11
-
-
74449093973
-
A comprehensive catalogue of somatic mutations from a human cancer genome
-
Pleasance E.D., Cheetham R.K., Stephens P.J., et al. A comprehensive catalogue of somatic mutations from a human cancer genome. Nature 2010, 463:191-196.
-
(2010)
Nature
, vol.463
, pp. 191-196
-
-
Pleasance, E.D.1
Cheetham, R.K.2
Stephens, P.J.3
-
12
-
-
72949119310
-
Complex landscapes of somatic rearrangement in human breast cancer genomes
-
Stephens P.J., McBride D.J., Lin M.L., et al. Complex landscapes of somatic rearrangement in human breast cancer genomes. Nature 2009, 462:1005-1010.
-
(2009)
Nature
, vol.462
, pp. 1005-1010
-
-
Stephens, P.J.1
McBride, D.J.2
Lin, M.L.3
-
13
-
-
79951497419
-
The genomic complexity of primary human prostate cancer
-
Berger M.F., Lawrence M.S., Demichelis F., et al. The genomic complexity of primary human prostate cancer. Nature 2011, 470:214-220.
-
(2011)
Nature
, vol.470
, pp. 214-220
-
-
Berger, M.F.1
Lawrence, M.S.2
Demichelis, F.3
-
14
-
-
79955555195
-
Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes
-
Hillmer A.M., Yao F., Inaki K., et al. Comprehensive long-span paired-end-tag mapping reveals characteristic patterns of structural variations in epithelial cancer genomes. Genome Res 2011, 21:665-675.
-
(2011)
Genome Res
, vol.21
, pp. 665-675
-
-
Hillmer, A.M.1
Yao, F.2
Inaki, K.3
-
15
-
-
78650909427
-
Limitations of next-generation genome sequence assembly
-
Alkan C., Sajjadian S., Eichler E.E. Limitations of next-generation genome sequence assembly. Nat Methods 2011, 8:61-65.
-
(2011)
Nat Methods
, vol.8
, pp. 61-65
-
-
Alkan, C.1
Sajjadian, S.2
Eichler, E.E.3
-
16
-
-
77954648699
-
High-resolution human genome structure by single-molecule analysis
-
Teague B., Waterman M.S., Goldstein S., et al. High-resolution human genome structure by single-molecule analysis. Proc Natl Acad Sci U S A 2010, 107:10848-10853.
-
(2010)
Proc Natl Acad Sci U S A
, vol.107
, pp. 10848-10853
-
-
Teague, B.1
Waterman, M.S.2
Goldstein, S.3
-
17
-
-
78649341898
-
Single molecule linear analysis of DNA in nano-channel labeled with sequence specific fluorescent probes
-
Das S.K., Austin M.D., Akana M.C., et al. Single molecule linear analysis of DNA in nano-channel labeled with sequence specific fluorescent probes. Nucleic Acids Res 2010, 38:e177.
-
(2010)
Nucleic Acids Res
, vol.38
-
-
Das, S.K.1
Austin, M.D.2
Akana, M.C.3
-
18
-
-
79952178131
-
High-quality draft assemblies of mammalian genomes from massively parallel sequence data
-
Gnerre S., Maccallum I., Przybylski D., et al. High-quality draft assemblies of mammalian genomes from massively parallel sequence data. Proc Natl Acad Sci U S A 2011, 108:1513-1518.
-
(2011)
Proc Natl Acad Sci U S A
, vol.108
, pp. 1513-1518
-
-
Gnerre, S.1
Maccallum, I.2
Przybylski, D.3
-
19
-
-
63849091245
-
Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses
-
Fullwood M.J., Wei C.L., Liu E.T., et al. Next-generation DNA sequencing of paired-end tags (PET) for transcriptome and genome analyses. Genome Res 2009, 19:521-532.
-
(2009)
Genome Res
, vol.19
, pp. 521-532
-
-
Fullwood, M.J.1
Wei, C.L.2
Liu, E.T.3
-
20
-
-
34250334695
-
Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs)
-
Ruan Y., Ooi H.S., Choo S.W., et al. Fusion transcripts and transcribed retrotransposed loci discovered through comprehensive transcriptome analysis using Paired-End diTags (PETs). Genome Res 2007, 17:828-838.
-
(2007)
Genome Res
, vol.17
, pp. 828-838
-
-
Ruan, Y.1
Ooi, H.S.2
Choo, S.W.3
-
21
-
-
43149125640
-
Scanning the human genome at kilobase resolution
-
Chen J., Kim Y.C., Jung Y.C., et al. Scanning the human genome at kilobase resolution. Genome Res 2008, 18:751-762.
-
(2008)
Genome Res
, vol.18
, pp. 751-762
-
-
Chen, J.1
Kim, Y.C.2
Jung, Y.C.3
-
22
-
-
22744453077
-
Exogenous AdoMet and its analogue sinefungin differentially influence DNA cleavage by R.EcoP15I-usefulness in SAGE
-
Raghavendra N.K., Rao D.N. Exogenous AdoMet and its analogue sinefungin differentially influence DNA cleavage by R.EcoP15I-usefulness in SAGE. Biochem Biophys Res Commun 2005, 334:803-811.
-
(2005)
Biochem Biophys Res Commun
, vol.334
, pp. 803-811
-
-
Raghavendra, N.K.1
Rao, D.N.2
-
23
-
-
62549131646
-
PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data
-
Korbel J.O., Abyzov A., Mu X.J., et al. PEMer: a computational framework with simulation-based error models for inferring genomic structural variants from massive paired-end sequencing data. Genome Biol 2009, 10:R23.
-
(2009)
Genome Biol
, vol.10
-
-
Korbel, J.O.1
Abyzov, A.2
Mu, X.J.3
-
24
-
-
69549116107
-
BreakDancer: an algorithm for high-resolution mapping of genomic structural variation
-
Chen K., Wallis J.W., McLellan M.D., et al. BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nat Methods 2009, 6:677-681.
-
(2009)
Nat Methods
, vol.6
, pp. 677-681
-
-
Chen, K.1
Wallis, J.W.2
McLellan, M.D.3
-
25
-
-
70350694443
-
Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads
-
Ye K., Schulz M.H., Long Q., et al. Pindel: a pattern growth approach to detect break points of large deletions and medium sized insertions from paired-end short reads. Bioinformatics 2009, 25:2865-2871.
-
(2009)
Bioinformatics
, vol.25
, pp. 2865-2871
-
-
Ye, K.1
Schulz, M.H.2
Long, Q.3
-
26
-
-
79551621409
-
ReadDepth: a Parallel R package for detecting copy number alterations from short sequencing reads
-
Miller C.A., Hampton O., Coarfa C., et al. ReadDepth: a Parallel R package for detecting copy number alterations from short sequencing reads. PLoS One 2011, 6:e16327.
-
(2011)
PLoS One
, vol.6
-
-
Miller, C.A.1
Hampton, O.2
Coarfa, C.3
-
27
-
-
0034831138
-
Segmental duplications: organization and impact within the current human genome project assembly
-
Bailey J.A., Yavor A.M., Massa H.F., et al. Segmental duplications: organization and impact within the current human genome project assembly. Genome Res 2001, 11:1005-1017.
-
(2001)
Genome Res
, vol.11
, pp. 1005-1017
-
-
Bailey, J.A.1
Yavor, A.M.2
Massa, H.F.3
-
28
-
-
59949091427
-
A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome
-
Hampton O.A., Den Hollander P., Miller C.A., et al. A sequence-level map of chromosomal breakpoints in the MCF-7 breast cancer cell line yields insights into the evolution of a cancer genome. Genome Res 2009, 19:167-177.
-
(2009)
Genome Res
, vol.19
, pp. 167-177
-
-
Hampton, O.A.1
Den Hollander, P.2
Miller, C.A.3
-
29
-
-
0037458031
-
Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics
-
Mootha V.K., Lepage P., Miller K., et al. Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proc Natl Acad Sci U S A 2003, 100:605-610.
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, pp. 605-610
-
-
Mootha, V.K.1
Lepage, P.2
Miller, K.3
-
31
-
-
62049085786
-
Transcriptome sequencing to detect gene fusions in cancer
-
Maher C.A., Kumar-Sinha C., Cao X., et al. Transcriptome sequencing to detect gene fusions in cancer. Nature 2009, 458:97-101.
-
(2009)
Nature
, vol.458
, pp. 97-101
-
-
Maher, C.A.1
Kumar-Sinha, C.2
Cao, X.3
-
32
-
-
79955560249
-
Transcriptional consequences of genomic structural aberrations in breast cancer
-
Inaki K., Hillmer A.M., Ukil L., et al. Transcriptional consequences of genomic structural aberrations in breast cancer. Genome Res 2011, 21:676-687.
-
(2011)
Genome Res
, vol.21
, pp. 676-687
-
-
Inaki, K.1
Hillmer, A.M.2
Ukil, L.3
-
33
-
-
60549092281
-
Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line
-
Zhao Q., Caballero O.L., Levy S., et al. Transcriptome-guided characterization of genomic rearrangements in a breast cancer cell line. Proc Natl Acad Sci U S A 2009, 106:1886-1891.
-
(2009)
Proc Natl Acad Sci U S A
, vol.106
, pp. 1886-1891
-
-
Zhao, Q.1
Caballero, O.L.2
Levy, S.3
-
34
-
-
65549165975
-
Genetic alterations and oncogenic pathways associated with breast cancer subtypes
-
Hu X., Stern H.M., Ge L., et al. Genetic alterations and oncogenic pathways associated with breast cancer subtypes. Mol Cancer Res 2009, 7:511-522.
-
(2009)
Mol Cancer Res
, vol.7
, pp. 511-522
-
-
Hu, X.1
Stern, H.M.2
Ge, L.3
-
35
-
-
17944376262
-
Comprehensive genome sequence analysis of a breast cancer amplicon
-
Collins C., Volik S., Kowbel D., et al. Comprehensive genome sequence analysis of a breast cancer amplicon. Genome Res 2001, 11:1034-1042.
-
(2001)
Genome Res
, vol.11
, pp. 1034-1042
-
-
Collins, C.1
Volik, S.2
Kowbel, D.3
-
36
-
-
27744434068
-
ZNF217 suppresses cell death associated with chemotherapy and telomere dysfunction
-
Huang G., Krig S., Kowbel D., et al. ZNF217 suppresses cell death associated with chemotherapy and telomere dysfunction. Hum Mol Genet 2005, 14:3219-3225.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 3219-3225
-
-
Huang, G.1
Krig, S.2
Kowbel, D.3
-
37
-
-
0037065939
-
Prognostic value of CCND1 gene status in sporadic breast tumours, as determined by real-time quantitative PCR assays
-
Bieche I., Olivi M., Nogues C., et al. Prognostic value of CCND1 gene status in sporadic breast tumours, as determined by real-time quantitative PCR assays. Br J Cancer 2002, 86:580-586.
-
(2002)
Br J Cancer
, vol.86
, pp. 580-586
-
-
Bieche, I.1
Olivi, M.2
Nogues, C.3
-
38
-
-
33847307543
-
Role of RAD51C and XRCC3 in genetic recombination and DNA repair
-
Liu Y., Tarsounas M., O'Regan P., et al. Role of RAD51C and XRCC3 in genetic recombination and DNA repair. J Biol Chem 2007, 282:1973-1979.
-
(2007)
J Biol Chem
, vol.282
, pp. 1973-1979
-
-
Liu, Y.1
Tarsounas, M.2
O'Regan, P.3
-
39
-
-
1242275403
-
Domain mapping of the Rad51 paralog protein complexes
-
Miller K.A., Sawicka D., Barsky D., et al. Domain mapping of the Rad51 paralog protein complexes. Nucleic Acids Res 2004, 32:169-178.
-
(2004)
Nucleic Acids Res
, vol.32
, pp. 169-178
-
-
Miller, K.A.1
Sawicka, D.2
Barsky, D.3
-
40
-
-
34447619477
-
Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer
-
Lewis A.G., Flanagan J., Marsh A., et al. Mutation analysis of FANCD2, BRIP1/BACH1, LMO4 and SFN in familial breast cancer. Breast Cancer Res 2005, 7:R1005-R1016.
-
(2005)
Breast Cancer Res
, vol.7
-
-
Lewis, A.G.1
Flanagan, J.2
Marsh, A.3
-
41
-
-
0142147272
-
The BRCT domain is a phospho-protein binding domain
-
Yu X., Chini C.C., He M., et al. The BRCT domain is a phospho-protein binding domain. Science 2003, 302:639-642.
-
(2003)
Science
, vol.302
, pp. 639-642
-
-
Yu, X.1
Chini, C.C.2
He, M.3
-
42
-
-
20644461718
-
BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function
-
Cantor S.B., Bell D.W., Ganesan S., et al. BACH1, a novel helicase-like protein, interacts directly with BRCA1 and contributes to its DNA repair function. Cell 2001, 105:149-160.
-
(2001)
Cell
, vol.105
, pp. 149-160
-
-
Cantor, S.B.1
Bell, D.W.2
Ganesan, S.3
-
43
-
-
34249950879
-
Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response
-
Kim H., Chen J., Yu X. Ubiquitin-binding protein RAP80 mediates BRCA1-dependent DNA damage response. Science 2007, 316:1202-1205.
-
(2007)
Science
, vol.316
, pp. 1202-1205
-
-
Kim, H.1
Chen, J.2
Yu, X.3
-
44
-
-
34547662882
-
CCDC98 targets BRCA1 to DNA damage sites
-
Liu Z., Wu J., Yu X. CCDC98 targets BRCA1 to DNA damage sites. Nat Struct Mol Biol 2007, 14:716-720.
-
(2007)
Nat Struct Mol Biol
, vol.14
, pp. 716-720
-
-
Liu, Z.1
Wu, J.2
Yu, X.3
-
45
-
-
58149216582
-
Germline RAP80 mutations and susceptibility to breast cancer
-
Akbari M.R., Ghadirian P., Robidoux A., et al. Germline RAP80 mutations and susceptibility to breast cancer. Breast Cancer Res Treat 2009, 113:377-381.
-
(2009)
Breast Cancer Res Treat
, vol.113
, pp. 377-381
-
-
Akbari, M.R.1
Ghadirian, P.2
Robidoux, A.3
-
46
-
-
68949092118
-
Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases
-
Novak D.J., Sabbaghian N., Maillet P., et al. Analysis of the genes coding for the BRCA1-interacting proteins, RAP80 and Abraxas (CCDC98), in high-risk, non-BRCA1/2, multiethnic breast cancer cases. Breast Cancer Res Treat 2009, 117:453-459.
-
(2009)
Breast Cancer Res Treat
, vol.117
, pp. 453-459
-
-
Novak, D.J.1
Sabbaghian, N.2
Maillet, P.3
-
47
-
-
84860244637
-
-
University of Michigan - Ann Arbor, U.S. Army Medical Research and Materiel Command
-
Yu X. Characterize RAP80, a potential tumor suppressor gene 2009, University of Michigan - Ann Arbor, U.S. Army Medical Research and Materiel Command, p. 24.
-
(2009)
Characterize RAP80, a potential tumor suppressor gene
, pp. 24
-
-
Yu, X.1
-
48
-
-
33845291140
-
Novel patterns of genome rearrangement and their association with survival in breast cancer
-
Hicks J., Krasnitz A., Lakshmi B., et al. Novel patterns of genome rearrangement and their association with survival in breast cancer. Genome Res 2006, 16:1465-1479.
-
(2006)
Genome Res
, vol.16
, pp. 1465-1479
-
-
Hicks, J.1
Krasnitz, A.2
Lakshmi, B.3
-
49
-
-
0043264447
-
Translocation and gross deletion breakpoints in human inherited disease and cancer I: nucleotide composition and recombination-associated motifs
-
Abeysinghe S.S., Chuzhanova N., Krawczak M., et al. Translocation and gross deletion breakpoints in human inherited disease and cancer I: nucleotide composition and recombination-associated motifs. Hum Mutat 2003, 22:229-244.
-
(2003)
Hum Mutat
, vol.22
, pp. 229-244
-
-
Abeysinghe, S.S.1
Chuzhanova, N.2
Krawczak, M.3
-
50
-
-
36448997332
-
Optimization of primer design for the detection of variable genomic lesions in cancer
-
Bashir A., Liu Y.T., Raphael B.J., et al. Optimization of primer design for the detection of variable genomic lesions in cancer. Bioinformatics 2007, 23:2807-2815.
-
(2007)
Bioinformatics
, vol.23
, pp. 2807-2815
-
-
Bashir, A.1
Liu, Y.T.2
Raphael, B.J.3
-
51
-
-
77950851118
-
Optimizing PCR assays for DNA-based cancer diagnostics.
-
Bashir A, Lu Q, Carson D, et al. Optimizing PCR assays for DNA-based cancer diagnostics. J Comput Biol;17:369-381.
-
J Comput Biol
, vol.17
, pp. 369-381
-
-
Bashir, A.1
Lu, Q.2
Carson, D.3
-
52
-
-
69649109364
-
Circos: an information aesthetic for comparative genomics
-
Krzywinski M., Schein J., Birol I., et al. Circos: an information aesthetic for comparative genomics. Genome Res 2009, 19:1639-1645.
-
(2009)
Genome Res
, vol.19
, pp. 1639-1645
-
-
Krzywinski, M.1
Schein, J.2
Birol, I.3
-
53
-
-
0036883717
-
Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer
-
Barlund M., Monni O., Weaver J.D., et al. Cloning of BCAS3 (17q23) and BCAS4 (20q13) genes that undergo amplification, overexpression, and fusion in breast cancer. Genes Chromosomes Cancer 2002, 35:311-317.
-
(2002)
Genes Chromosomes Cancer
, vol.35
, pp. 311-317
-
-
Barlund, M.1
Monni, O.2
Weaver, J.D.3
-
54
-
-
64849111009
-
Clinical significance of miR-21 expression in breast cancer: SYBR-Green I-based real-time RT-PCR study of invasive ductal carcinoma
-
Huang G.L., Zhang X.H., Guo G.L., et al. Clinical significance of miR-21 expression in breast cancer: SYBR-Green I-based real-time RT-PCR study of invasive ductal carcinoma. Oncol Rep 2009, 21:673-679.
-
(2009)
Oncol Rep
, vol.21
, pp. 673-679
-
-
Huang, G.L.1
Zhang, X.H.2
Guo, G.L.3
-
55
-
-
48849086912
-
Deciphering downstream gene targets of PI3K/mTOR/p70S6K pathway in breast cancer
-
Heinonen H., Nieminen A., Saarela M., et al. Deciphering downstream gene targets of PI3K/mTOR/p70S6K pathway in breast cancer. BMC Genomics 2008, 9:348.
-
(2008)
BMC Genomics
, vol.9
, pp. 348
-
-
Heinonen, H.1
Nieminen, A.2
Saarela, M.3
-
56
-
-
70350244514
-
Novel lipogenic enzyme ELOVL7 is involved in prostate cancer growth through saturated long-chain fatty acid metabolism
-
Tamura K., Makino A., Hullin-Matsuda F., et al. Novel lipogenic enzyme ELOVL7 is involved in prostate cancer growth through saturated long-chain fatty acid metabolism. Cancer Res 2009, 69:8133-8140.
-
(2009)
Cancer Res
, vol.69
, pp. 8133-8140
-
-
Tamura, K.1
Makino, A.2
Hullin-Matsuda, F.3
-
57
-
-
1042280961
-
Multi-species comparative mapping in silico using the COMPASS strategy
-
Liu L., Gong G., Liu Y., et al. Multi-species comparative mapping in silico using the COMPASS strategy. Bioinformatics 2004, 20:148-154.
-
(2004)
Bioinformatics
, vol.20
, pp. 148-154
-
-
Liu, L.1
Gong, G.2
Liu, Y.3
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